Any hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the MYL2 gene.
Comprehensive, easy-to-understand information about this condition
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Gene data from MyGene.info • Click to view on NCBI Gene
hypertrophic cardiomyopathy 2
MONDO:0007266
hypertrophic cardiomyopathy 3
MONDO:0007267
hypertrophic cardiomyopathy 4
MONDO:0007268
Beckwith-Wiedemann syndrome
MONDO:0007534
myotonic dystrophy type 1
MONDO:0008056
hypertrophic cardiomyopathy 1
MONDO:0008647